Allopurinol Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9533

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Allopurinol Sodium (NDC 0143-9533). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Allopurinol Sodium For Injection 1)

FDA Label Image

Allopurinol Sodium For Injection Vial Label (Allopurinol Sodium For Injection 2)

Allopurinol Sodium For Injection Vial Label (Allopurinol Sodium For Injection 2)
This is a description of a medication with the NDC code 0143-9533-01. It is to be prepared as a sterile solution for injection into a vial and should be swirled until properly mixed. It contains allopurinol sodium for intravenous infusion and each vial contains 500 mg of allopurinol. The temperature at which it should be stored is between 20° to 25° (668° to 77°F) and administration should begin promptly. More detailed instructions and precautions are included on the package insert. There is some illegible text that makes it difficult to provide a complete description.*
FDA Label Image

Allopurinol Sodium For Injection 3

Allopurinol Sodium For Injection 3
This appears to be the package insert for Allopurinol Sodium, a medication that is administered through intravenous infusion. It comes as a sterile single-use vial, and the dosage and administration instructions are provided. The manufacturer is Hikma Pharmaceuticals.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.